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嗜水气单胞菌LuxR同源物AhyR以生长阶段依赖性方式正向和负向调节N-酰基高丝氨酸内酯合酶AhyI。

The Aeromonas hydrophila LuxR homologue AhyR regulates the N-acyl homoserine lactone synthase, AhyI positively and negatively in a growth phase-dependent manner.

作者信息

Kirke David F, Swift Simon, Lynch Martin J, Williams Paul

机构信息

Centre for Biomolecular Sciences, Institute of Infection, Immunity and Inflammation, University of Nottingham, Nottingham NG7 2RD, UK.

出版信息

FEMS Microbiol Lett. 2004 Dec 1;241(1):109-17. doi: 10.1016/j.femsle.2004.10.011.

Abstract

Aeromonas hydrophila is a pathogen of fish, amphibians and humans which produces N-acylhomoserine lactone quorum sensing signal molecules and possesses homologues of the Vibrio fischeri luxI and luxR quorum sensing genes termed ahyI and ahyR, respectively. The ahyI and ahyR genes of A. hydrophila comprise a divergon with a 62 bp intergenic region and control biofilm maturation and extracellular protease production. Stationary phase culture supernatants from an ahyR but not an ahyI mutant contain N-butanoylhomoserine lactone (C4-HSL) which is shown to be required for maximal ahyI expression. To determine whether AhyR regulates ahyI, the expression of AhyI was followed throughout growth by Western blot analysis. This revealed that AhyI can be detected in the exponential phase but appears to be degraded in stationary phase in the parent A. hydrophila strain. In an ahyR mutant however, the AhyI protein is only produced in stationary phase but production is sustained suggesting that AhyR controls the timing of AhyI production and turnover. By using RT-PCR, we mapped the transcriptional start site of ahyI which revealed that the 12 bp symmetrical lux-box like sequence present in the 62 bp ahyRI intergenic region overlaps with the -10 region of the ahyI promoter. To determine whether AhyR could bind to the ahyRI intergenic region, the ahyR gene was expressed and purified as a maltose binding protein (MalE) fusion. Electrophoretic mobility shift assays demonstrated that MalE-AhyR specifically bound to this sequence in both the presence and absence of N-butanoylhomoserine lactone (C4-HSL). Taken together, these data suggest that AhyR acts as both a negative and a positive regulator of ahyI and hence C4-HSL production in a growth phase dependent manner.

摘要

嗜水气单胞菌是鱼类、两栖动物和人类的病原体,它能产生N-酰基高丝氨酸内酯群体感应信号分子,并且拥有分别被称为ahyI和ahyR的费氏弧菌luxI和luxR群体感应基因的同源物。嗜水气单胞菌的ahyI和ahyR基因组成一个具有62 bp基因间区域的发散操纵子,控制生物膜成熟和细胞外蛋白酶的产生。来自ahyR突变体而非ahyI突变体的稳定期培养上清液含有N-丁酰高丝氨酸内酯(C4-HSL),这被证明是最大程度ahyI表达所必需的。为了确定AhyR是否调节ahyI,通过蛋白质免疫印迹分析追踪整个生长过程中AhyI的表达。这表明在指数期可以检测到AhyI,但在嗜水气单胞菌亲本菌株的稳定期似乎会被降解。然而,在ahyR突变体中,AhyI蛋白仅在稳定期产生,但产量持续存在,这表明AhyR控制AhyI产生和周转的时间。通过使用逆转录聚合酶链反应(RT-PCR),我们确定了ahyI的转录起始位点,结果显示在62 bp的ahyRI基因间区域中存在的12 bp对称lux-box样序列与ahyI启动子的-10区域重叠。为了确定AhyR是否能与ahyRI基因间区域结合,ahyR基因作为麦芽糖结合蛋白(MalE)融合蛋白进行表达和纯化。电泳迁移率变动分析表明,无论是否存在N-丁酰高丝氨酸内酯(C4-HSL),MalE-AhyR都能特异性结合该序列。综上所述,这些数据表明AhyR以生长阶段依赖的方式作为ahyI以及因此C4-HSL产生的负调节因子和正调节因子。

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